Overview

Variant ID 1161
Entrez Gene ID 79934
Gene ADCK4 (GeneCards)
Location hg19 19:41206317-41206317
hg38 19:40700412-40700412
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500 v2
Mutation(HGVS format) NC_000019.9:g.41206317_41206317 del (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NM_024876.3
mRNA length 2458
Reference length 59128983

Annotations and predictions

Deleterious probability by DeFine 0.9408 (Deleterious)
Entrez Gene ID 79934 (NCBI Gene)
Official Gene Symbol ADCK4 (GeneCards)
Number of variants in COQ8B in this database 2 (view all the variants)
Full name coenzyme Q8B
Band 19q13.2
Other IDs Vega: OTTHUMG00000182620
OMIM: 615567
HGNC: HGNC:19041
Ensembl: ENSG00000123815
Other names ADCK4, NPHS9
Summary This gene encodes a protein with two copies of a domain found in protein kinases. The encoded protein has a complete protein kinase catalytic domain, and a truncated domain that contains only the active and binding sites of the protein kinase domain, however, it is not known whether the protein has any kinase activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]

Individual #1

Individual ID 28867142.33 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Male Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;